Variant report

Variant	rs16942475
Chromosome Location	chr17:46688371-46688372
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PML	chr17:46687581-46688690	GM12878	blood:	n/a	n/a
2	TAF1	chr17:46688335-46688611	GM12878	blood:	n/a	n/a
3	USF1	chr17:46688302-46688552	HepG2	liver:	n/a	chr17:46688414-46688425 chr17:46688400-46688411
4	E2F6	chr17:46687436-46688997	A549	lung:	n/a	chr17:46687709-46687718 chr17:46687918-46687930 chr17:46687619-46687628 chr17:46687785-46687800
5	POLR2A	chr17:46687386-46688986	HCT-116	colon:	n/a	n/a
6	SP1	chr17:46687602-46688986	A549	lung:	n/a	chr17:46687618-46687630 chr17:46688409-46688418 chr17:46687708-46687720 chr17:46687710-46687719 chr17:46688410-46688419 chr17:46687710-46687719 chr17:46688409-46688419 chr17:46688408-46688420 chr17:46688408-46688420 chr17:46688409-46688419 chr17:46687620-46687629 chr17:46688409-46688418 chr17:46687619-46687628 chr17:46687794-46687801 chr17:46687705-46687719 chr17:46687709-46687718
7	MAX	chr17:46687345-46689850	A549	lung:	n/a	chr17:46689596-46689606 chr17:46687379-46687389 chr17:46688399-46688412 chr17:46688400-46688411 chr17:46688415-46688424 chr17:46687617-46687627 chr17:46688401-46688410 chr17:46688401-46688410 chr17:46688413-46688422 chr17:46688414-46688425 chr17:46689593-46689603 chr17:46688401-46688410 chr17:46688399-46688412 chr17:46688400-46688409
8	CHD2	chr17:46688317-46688521	K562	blood:	n/a	n/a
9	GTF2F1	chr17:46688080-46689248	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr17:46687211-46689612	ProgFib	skin:	n/a	n/a
11	YY1	chr17:46688299-46688703	A549	lung:	n/a	chr17:46688427-46688436 chr17:46688546-46688557
12	SMARCC2	chr17:46687761-46688649	Hela-S3	cervix:	n/a	n/a
13	ELF1	chr17:46687463-46688907	MCF-7	breast:	n/a	chr17:46687838-46687850
14	USF2	chr17:46688172-46688600	K562	blood:	n/a	chr17:46688413-46688424 chr17:46688565-46688581 chr17:46688400-46688411
15	POLR2A	chr17:46687477-46689378	HUVEC	blood vessel:	n/a	n/a
16	TAF1	chr17:46687346-46688984	A549	lung:	n/a	n/a
17	MAX	chr17:46688215-46688605	HUVEC	blood vessel:	n/a	chr17:46688399-46688412 chr17:46688400-46688411 chr17:46688415-46688424 chr17:46688401-46688410 chr17:46688401-46688410 chr17:46688413-46688422 chr17:46688414-46688425 chr17:46688401-46688410 chr17:46688399-46688412 chr17:46688400-46688409
18	USF1	chr17:46688026-46688529	GM12878	blood:	n/a	chr17:46688414-46688425 chr17:46688400-46688411
19	POLR2A	chr17:46687624-46688859	Raji	blood:	n/a	n/a
20	ATF3	chr17:46688217-46688585	K562	blood:	n/a	chr17:46688409-46688429
21	MAX	chr17:46687514-46688778	Hela-S3	cervix:	n/a	chr17:46688399-46688412 chr17:46688400-46688411 chr17:46688415-46688424 chr17:46687617-46687627 chr17:46688401-46688410 chr17:46688401-46688410 chr17:46688413-46688422 chr17:46688414-46688425 chr17:46688401-46688410 chr17:46688399-46688412 chr17:46688400-46688409
22	TAF1	chr17:46688228-46688637	A549	lung:	n/a	n/a
23	SIX5	chr17:46687838-46688891	A549	lung:	n/a	n/a
24	POLR2A	chr17:46687601-46688549	GM12878	blood:	n/a	n/a
25	USF1	chr17:46687436-46689840	HCT-116	colon:	n/a	chr17:46688414-46688425 chr17:46688565-46688581 chr17:46688400-46688411
26	BHLHE40	chr17:46688243-46688503	K562	blood:	n/a	n/a
27	POLR2A	chr17:46687462-46688390	GM12892	blood:	n/a	n/a
28	POLR2A	chr17:46687562-46688622	GM12878	blood:	n/a	n/a
29	JUND	chr17:46687507-46688800	A549	lung:	n/a	n/a
30	USF1	chr17:46687908-46688741	A549	lung:	n/a	chr17:46688414-46688425 chr17:46688565-46688581 chr17:46688400-46688411
31	MAX	chr17:46687768-46688683	MCF-7	breast:	n/a	chr17:46688399-46688412 chr17:46688400-46688411 chr17:46688415-46688424 chr17:46688401-46688410 chr17:46688401-46688410 chr17:46688413-46688422 chr17:46688414-46688425 chr17:46688401-46688410 chr17:46688399-46688412 chr17:46688400-46688409
32	USF1	chr17:46688182-46688593	SK-N-SH_RA	brain:	n/a	chr17:46688414-46688425 chr17:46688565-46688581 chr17:46688400-46688411
33	ELK1	chr17:46687716-46688548	Hela-S3	cervix:	n/a	n/a
34	MAX	chr17:46687820-46688571	K562	blood:	n/a	chr17:46688399-46688412 chr17:46688400-46688411 chr17:46688415-46688424 chr17:46688401-46688410 chr17:46688401-46688410 chr17:46688413-46688422 chr17:46688414-46688425 chr17:46688401-46688410 chr17:46688399-46688412 chr17:46688400-46688409
35	YY1	chr17:46687900-46688737	HCT-116	colon:	n/a	chr17:46688427-46688436 chr17:46688546-46688557
36	SIN3AK20	chr17:46687005-46689014	PANC-1	pancreas:	n/a	n/a
37	POLR2A	chr17:46686211-46690442	SK-N-MC	brain:	n/a	n/a
38	TBP	chr17:46687754-46688630	K562	blood:	n/a	n/a
39	POLR2A	chr17:46687368-46688803	HUVEC	blood vessel:	n/a	n/a
40	USF1	chr17:46687996-46688664	SK-N-SH	brain:	n/a	chr17:46688414-46688425 chr17:46688565-46688581 chr17:46688400-46688411
41	MAX	chr17:46687054-46691101	A549	lung:	n/a	chr17:46689596-46689606 chr17:46687379-46687389 chr17:46688399-46688412 chr17:46688400-46688411 chr17:46688415-46688424 chr17:46687617-46687627 chr17:46688401-46688410 chr17:46688401-46688410 chr17:46688413-46688422 chr17:46688414-46688425 chr17:46689593-46689603 chr17:46688401-46688410 chr17:46688399-46688412 chr17:46687253-46687263 chr17:46688400-46688409
42	USF1	chr17:46687961-46688722	H1-hESC	embryonic stem cell:	n/a	chr17:46688414-46688425 chr17:46688565-46688581 chr17:46688400-46688411
43	YY1	chr17:46687534-46688617	GM12878	blood:	n/a	chr17:46687709-46687718 chr17:46688427-46688436 chr17:46688546-46688557
44	CREB1	chr17:46688276-46688733	A549	lung:	n/a	n/a
45	FOS	chr17:46688205-46688608	GM12878	blood:	n/a	n/a
46	FOSL2	chr17:46688063-46688448	A549	lung:	n/a	n/a
47	HA-E2F1	chr17:46687654-46688410	MCF-7	breast:	n/a	chr17:46687709-46687718 chr17:46687947-46687958 chr17:46687785-46687800
48	POLR2A	chr17:46687550-46688788	K562	blood:	n/a	n/a
49	USF1	chr17:46687907-46688888	A549	lung:	n/a	chr17:46688414-46688425 chr17:46688565-46688581 chr17:46688400-46688411
50	TAF1	chr17:46687506-46688688	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46688329-46688379	BJ	skin:	n/a
2	chr17:46688329-46688379	PFSK-1	brain:	n/a
3	chr17:46688329-46688379	SK-N-SH	brain:	n/a
4	chr17:46688321-46688371	MCF-7	breast:	n/a
5	chr17:46688329-46688379	T-47D	breast:	n/a
6	chr17:46688321-46688371	HCT-116	colon:	n/a
7	chr17:46688321-46688371	GM06990	blood:	n/a
8	chr17:46688321-46688371	HMEC	breast:	n/a
9	chr17:46688321-46688371	HRPEpiC	eye:	n/a
10	chr17:46688329-46688379	HRCEpiC	kidney:	n/a
11	chr17:46688321-46688371	PFSK-1	brain:	n/a
12	chr17:46688321-46688371	NHDF-neo	bronchial:	n/a
13	chr17:46688321-46688371	ovcar-3	ovarian:	n/a
14	chr17:46688329-46688379	HIPEpiC	eye:	n/a
15	chr17:46688321-46688371	IMR90	lung:	fetal
16	chr17:46688321-46688371	SKMC	muscle:	n/a
17	chr17:46688321-46688371	NB4	blood:	n/a
18	chr17:46688329-46688379	IMR90	lung:	fetal
19	chr17:46688321-46688371	SK-N-SH	brain:	n/a
20	chr17:46688329-46688379	NHDF-neo	bronchial:	n/a
21	chr17:46688321-46688371	Caco-2	colon:	n/a
22	chr17:46688329-46688379	GM12892	blood:	n/a
23	chr17:46688321-46688371	AG09319	gingival:	n/a
24	chr17:46688321-46688371	HNPCEpiC	eye:	n/a
25	chr17:46688321-46688371	HUVEC	blood vessel:	n/a
26	chr17:46688321-46688371	MCF10A-Er-Src	breast:	n/a
27	chr17:46688321-46688371	HCM	heart:	n/a
28	chr17:46688329-46688379	BE2_C	brain:	n/a
29	chr17:46688321-46688371	SAEC	small airway:	n/a
30	chr17:46688321-46688371	AoSMC	blood vessel:	n/a
31	chr17:46688329-46688379	HCT-116	colon:	n/a
32	chr17:46688329-46688379	GM12878	blood:	n/a
33	chr17:46688321-46688371	GM12878	blood:	n/a
34	chr17:46688329-46688379	MCF-7	breast:	n/a
35	chr17:46688321-46688371	AG04449	skin:	fetal
36	chr17:46688329-46688379	K562	blood:	n/a
37	chr17:46688329-46688379	Hepatocyte	liver:	n/a
38	chr17:46688329-46688379	AG04450	lung:	fetal
39	chr17:46688329-46688379	ProgFib	skin:	n/a
40	chr17:46688329-46688379	Jurkat	blood:	n/a
41	chr17:46688321-46688371	HCF	heart:	n/a
42	chr17:46688329-46688379	MCF10A-Er-Src	breast:	n/a
43	chr17:46688329-46688379	SK-N-MC	brain:	n/a
44	chr17:46688321-46688371	AG10803	skin:	n/a
45	chr17:46688321-46688371	NHBE	bronchial:	n/a
46	chr17:46688321-46688371	NH-A	brain:	n/a
47	chr17:46688329-46688379	NHBE	bronchial:	n/a
48	chr17:46688329-46688379	LNCaP	prostate:	n/a
49	chr17:46688329-46688379	AG04449	skin:	fetal
50	chr17:46688321-46688371	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:62608963..62609484-chr17:46687712..46688537,2	Hela-S3	cervix:
2	chr17:46687246..46688797-chr17:46690963..46692920,2	MCF-7	breast:
3	chr17:42276914..42277853-chr17:46688189..46688726,2	Hela-S3	cervix:
4	chr17:46685746..46689281-chr17:46702801..46705653,3	MCF-7	breast:
5	chr17:46123851..46125972-chr17:46688272..46690385,2	MCF-7	breast:
6	chr17:46675371..46683952-chr17:46685648..46690575,16	MCF-7	breast:
7	chr14:70234049..70234581-chr17:46688359..46689314,2	Hela-S3	cervix:
8	chr17:46686493..46690300-chr17:46702976..46707350,6	MCF-7	breast:

Variant related genes	Relation type
HOXB7	TF binding region
HOXB7	CpG island
ENSG00000120093	Chromatin interaction
ENSG00000082641	Chromatin interaction
ENSG00000120068	Chromatin interaction
ENSG00000100650	Chromatin interaction
ENSG00000108511	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000263412	Chromatin interaction
ENSG00000170689	Chromatin interaction
ENSG00000242207	Chromatin interaction
ENSG00000087152	Chromatin interaction
ENSG00000233101	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs15689	0.89[JPT][hapmap]
rs2277696	1.00[CEU][hapmap]
rs2288280	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs2303485	0.80[EUR][1000 genomes]
rs3744776	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[GIH][hapmap];0.89[JPT][hapmap]
rs3786138	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55711449	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs919109	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833469	chr17:46491849-46709406	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
2	esv3420538	chr17:46504944-46861553	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	369 gene(s)	inside rSNPs	diseases
3	nsv908577	chr17:46584900-46704536	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	343 gene(s)	inside rSNPs	diseases
4	nsv908578	chr17:46592413-46698710	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
5	nsv908579	chr17:46592413-46727289	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
6	nsv532113	chr17:46598247-47588570	Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	453 gene(s)	inside rSNPs	diseases
7	esv2758459	chr17:46602673-46836837	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
8	esv2758694	chr17:46602673-46836837	Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
9	nsv908580	chr17:46609103-46698710	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
10	nsv908581	chr17:46610646-46735520	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
11	nsv908582	chr17:46617019-46698710	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
12	nsv908583	chr17:46617019-46704536	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
13	nsv833471	chr17:46617787-46783345	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	356 gene(s)	inside rSNPs	diseases
14	nsv908584	chr17:46618926-46735520	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
15	nsv457822	chr17:46620402-46698710	Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
16	nsv575481	chr17:46620402-46698710	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
17	nsv457823	chr17:46620402-46704536	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
18	nsv575482	chr17:46620402-46704536	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
19	nsv457824	chr17:46625519-46693491	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
20	nsv575483	chr17:46625519-46693491	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
21	nsv543380	chr17:46686151-46721371	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46683600-46691000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr17:46687000-46688600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
3	chr17:46687000-46689000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr17:46687000-46689000	Active TSS	Fetal Kidney	kidney
5	chr17:46687000-46690400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
6	chr17:46687000-46691600	Active TSS	HSMMtube	muscle
7	chr17:46687200-46688600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr17:46687200-46688600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
9	chr17:46687200-46688600	Active TSS	NHLF	lung
10	chr17:46687200-46688800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
11	chr17:46687200-46689000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
12	chr17:46687200-46689000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
13	chr17:46687200-46689200	Active TSS	Right Atrium	heart
14	chr17:46687200-46689200	Active TSS	Hela-S3	cervix
15	chr17:46687200-46689200	Active TSS	HSMM	muscle
16	chr17:46687200-46689600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
17	chr17:46687200-46690400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
18	chr17:46687200-46692800	Active TSS	NHDF-Ad	bronchial
19	chr17:46687400-46688400	Flanking Bivalent TSS/Enh	HepG2	liver
20	chr17:46687400-46688600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr17:46687400-46688600	Active TSS	Small Intestine	intestine
22	chr17:46687400-46688800	Flanking Bivalent TSS/Enh	Thymus	Thymus
23	chr17:46687400-46689000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
24	chr17:46687400-46689000	Active TSS	Aorta	Aorta
25	chr17:46687400-46689000	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
26	chr17:46687400-46689000	Flanking Bivalent TSS/Enh	Placenta	Placenta
27	chr17:46687400-46689000	Active TSS	Rectal Smooth Muscle	rectum
28	chr17:46687400-46689200	Bivalent/Poised TSS	Fetal Lung	lung
29	chr17:46687400-46689200	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr17:46687400-46689200	Active TSS	Sigmoid Colon	Sigmoid Colon
31	chr17:46687400-46689200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
32	chr17:46687400-46689400	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
33	chr17:46687400-46690200	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
34	chr17:46687400-46691000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr17:46687400-46692400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr17:46687400-46692400	Active TSS	A549	lung
37	chr17:46687400-46692800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr17:46687600-46688400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
39	chr17:46687600-46688600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr17:46687600-46688600	Active TSS	Muscle Satellite Cultured Cells	--
41	chr17:46687600-46688600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr17:46687600-46688600	Flanking Bivalent TSS/Enh	HMEC	breast
43	chr17:46687600-46688800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr17:46687600-46688800	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
45	chr17:46687600-46688800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
46	chr17:46687600-46688800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr17:46687600-46688800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
48	chr17:46687600-46689000	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
49	chr17:46687600-46689000	Bivalent/Poised TSS	Fetal Brain Female	brain
50	chr17:46687600-46689000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus

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